Flame retardant retroreflective film structure

ABSTRACT

Flame retardant and heat resistant retroreflective structures are disclosed. Generally, the retroreflective structure includes a transparent plasticized polyvinyl chloride film, an array of retroreflective cube-corner elements underlying the transparent plasticized polyvinyl chloride film, a flame retardant and heat resistant adhesive underlying the array of retroreflective cube-corner elements, and a flame retardant woven fabric bonded to the flame retardant and heat resistant adhesive.

RELATED APPLICATION

This application claims the benefit of U.S. Provisional PatentApplication No. 60/782,347, filed on Mar. 15, 2006, the entire teachingsof which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

Retroreflective materials are employed for various safety and decorativepurposes. Particularly, these materials are useful at nighttime whenvisibility is important under low light conditions. With perfectretroreflective materials, light rays are reflected essentially towardsa light source in a substantially parallel path along an axis ofretroreflectivity. Retroreflective materials can be used as reflectivetapes and patches for clothing, such as vests and belts. Also,retroreflective materials can be used on posts, barrels, traffic conecollars, highway signs, vehicles, warning reflectors, etc.Retroreflective material can include arrays of randomly oriented microndiameter spheres or close packed cube-corner (prismatic) arrays.

Cube-corner or prismatic retroreflectors are described, for example, inU.S. Pat. No. 3,712,706, issued to Stamm on Jan. 23, 1973, the teachingsof which are incorporated by reference herein. Generally, the prisms canbe made by forming a master negative die on a flat surface of a metalplate or other suitable material. To form grooves 60 degrees apart areinscribed in the flat plate. The die is then used to process the desiredcube-corner array into a rigid flat plastic surface.

Further details concerning the structures and operation of cube-cornermicroprisms can be found in U.S. Pat. No. 3,684,348, issued to Rowlandon Aug. 15, 1972, the teachings of which are incorporated by referenceherein. A method for making retroreflective sheeting is also disclosedin U.S. Pat. No. 3,689,346 issued to Rowland on Sep. 5, 1972, theteachings of which are incorporated by reference herein. For example,cube-corner microprisms can be formed in a cooperatively configuredmold. The prisms can be bonded to sheeting, which is applied thereoverto provide a composite structure in which the cube-corner elementsproject from one surface of the sheeting.

Retroreflective materials can be particularly useful when visibility iscritical such as under emergency conditions. For example,retroreflective materials can be used for firefighters' coats andprotective clothing. However, the conditions that firefighters areexposed to can be harsh, especially in regard to excessive heat andtemperature conditions. Many retroreflective materials are made ofplastics that soften at temperatures of about 100° C. The softenedplastic in such materials can begin to flow causing the material to loseits retroreflectivity and thereby impair visibility. The National FireProtection Association (NFPA) has established standards that can be usedto evaluate clothing and retroreflective structures intended to be wornby firefighters.

SUMMARY OF THE INVENTION

The present invention is directed to flame retardant and heat resistantretroreflective structures. In one embodiment, the retroreflectivestructure includes a transparent plasticized polyvinyl chloride film, anarray of retroreflective cube-corner elements underlying the transparentplasticized polyvinyl chloride film, a flame retardant and heatresistant adhesive underlying the array of retroreflective cube-cornerelements; and a flame retardant woven fabric bonded to the flameretardant and heat resistant adhesive.

In other embodiments, retroreflective structures include a transparentplasticized polyvinyl chloride film; an array of retroreflectivecube-corner elements underlying the transparent plasticized polyvinylchloride film, a metallized reflective layer deposited on theretroreflective cube-corner elements, a flame retardant and heatresistant crosslinked acrylic adhesive bonded to the metallizedreflective layer, and a flame retardant woven fabric bonded to theacrylic adhesive.

The retroreflective structures described herein can meet or exceedstandards set by the NFPA for application to firefighters' clothing.Advantageously, retroreflective structures of the present invention caninclude a plasticized polyvinyl chloride film that does not need tocontain fire retardant additives in order to meet NFPA standards.Consequently, conventional, off-the-shelf plasticized polyvinvylchloride films can be used to make the retroreflective structures.Further, the retroreflective structures can include an array ofcube-corner elements that also does not need to contain fire retardantadditives in order to meet NFPA standards for the retroreflectivestructures. In addition, in some embodiments, the retroreflectivestructures can meet NFPA standards without having additional layers,e.g., overlying the plasticized polyvinyl chloride film, which containfire retardant additives.

The flame retardant feature of the present invention allows the productto be utilized for applications where flame resistance is required ordesirable.

In some embodiments, the heat resistant feature of the present inventionprevents melting or dripping, for example, at temperatures up to about260° C. for about 5 minutes. In addition, the retroreflective structuresof the present invention can be heated to about 140° C. for about 10minutes while maintaining at least about 100 SIA retroreflectivity.

The present invention can be used on firefighter's turnout gear toimprove conspicuousness, for example, during wet conditions or at dawn,dusk, and nighttime. In particular, the invention can be slit into tapeswhereby the tapes are sewn to the firefighter's turnout gear. Inaddition, the product can be used for other applications wherebyconspicuousness, heat resistance, and flame retardancy are desired ornecessary.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other objects, features and advantages of theinvention will be apparent from the following more particulardescription of preferred embodiments of the invention, as illustrated inthe accompanying drawings in which like reference characters refer tothe same parts throughout the different views. The drawings are notnecessarily to scale, emphasis instead being placed upon illustratingthe principles of the invention.

FIG. 1 is a cross sectional view of a retroreflective structure formedaccording to one embodiment of the present invention.

FIG. 2 is a cross sectional view of a retroreflective structure,containing optional transparent coatings, according to anotherembodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

A description of preferred embodiments of the invention follows.

Generally, the retroreflective structures of the present inventioninclude a transparent plasticized polyvinyl chloride film, an array ofretroreflective cube-corner elements underlying the transparentplasticized polyvinyl chloride film, a flame retardant and heatresistant adhesive underlying the array of retroreflective cube-cornerelements; and a flame retardant woven fabric bonded to the flameretardant and heat resistant adhesive.

FIGS. 1 and 2 illustrate embodiments of the present invention.Retroreflective structures 10 and 22 include transparent plasticizedpolyvinyl chloride film 12. Suitable transparent plasticized vinyl filmscan be manufactured, for example, by calendaring, extrusion, solventcasting, or other methods known in the art. Polyvinyl chloride film 12can contain various colorants and performance additives well-known tothose of skill in the art. In a preferred embodiment, the film is acalendered film. Calendaring can be an especially useful method due tothe flexibility of the calendaring process to compound colorants andperformance enhancement additives.

Polyvinyl chloride film 12 is substantially transparent. In someembodiments, Polyvinyl chloride film 12 is substantially transparent tovisible light. Polyvinyl chloride film 12 can be either clear ortransparently colored. In some embodiments, the polyvinyl chloride filmincludes a fluorescent dye. Retroreflective structures of the presentinvention can include a plasticized polyvinyl chloride film that doesnot need to contain fire retardant additives in order to meet NFPAstandards. Consequently, in some embodiments, the plasticized polyvinylchloride film is essentially free of fire retardant additives.

Polyvinyl chloride film 12 can have a thickness, for example, of about0.001 to about 0.022 inches (about 0.025 mm to about 0.56 mm) such asabout 0.004 to about 0.020 inches (about 0.1 millimeters (mm) to about0.51 mm), about 0.004 to about 0.01 inches (about 0.1 mm to about 0.25mm), about 0.006 to about 0.01 inches (about 0.15 mm to about 0.25 mm),or about 0.006 to about 0.018 inches (about 0.15 mm to about 0.46 mm).The thickness of the base film can be selected based on the flexibility,tear resistance, and color stability desired for any particularapplication. Furthermore, the selected film thickness of the structurecan be selected based on the desired long-term weatherabilitycharacteristics of the structure. In general, thinner layers ofpolyvinyl chloride films are preferred to further limit flammability ofthe retroreflective structure. For example, in preferred embodiments,the polyvinyl chloride film has a thickness about 0.004 to about 0.01inches (about 0.1 mm to about 0.25 mm).

The transparent plasticized polyvinyl chloride film has a Shore Ahardness, for example, of about 25 to about 60 such as about 30 to about50, about 30 to about 45, or about 35 to about 40. In one particularembodiment, the transparent plasticized polyvinyl chloride film has aShore A hardness of about 36. Shore A hardness is a measure of therelative hardness of a material and can be determined with an instrumentcalled a Shore A durometer.

Examples of suitable polyvinyl chloride film include a polyvinylchloride film available from American Renolit Corporation under thetrademark RENOLIT® (Whippany, N.J.), or a calendered plasticizedpolyvinyl chloride film available from Achilles USA, Everett, Wash.

In addition to polyvinyl chloride film 12, the retroreflectivestructures also include an array of retroreflective cube-cornerelements. Generally, the retroreflective structure includes array ofretroreflective cube-corner elements 14 underlying transparentplasticized polyvinyl chloride film 12. “Underlying” refers to therelative orientation of the retroreflective cube-corner elements to thetransparent plasticized polyvinyl chloride film.

The polyvinyl chloride film can provide a substrate for an array ofretroreflective cube-corner elements. In one embodiment, the array ofretroreflective cube-corner elements is attached to the polyvinylchloride film. Generally, the array of retroreflective cube-cornerelements has a window side exposed to incoming light rays and anopposite, facet side. The array of retroreflective cube-corner elementscan be oriented such that the window side faces the polyvinyl chloridefilm. For example, window side of the array of retroreflectivecube-corner elements can be attached to the polyvinyl chloride film. Insome embodiments, the array of retroreflective cube-corner elements isattached to the polyvinyl chloride film using a transparent adhesive.Alternatively, the array of retroreflective cube-corner elements can beattached to the polyvinyl chloride film using a transparent coating,described further infra, such as a transparent coating formed from aradiation-curable or solvent or water based coating formulation. In oneembodiment, the array of retroreflective cube-corner elements can becast directly onto the polyvinyl chloride film.

Array of retroreflective cube-corner elements 14 can be formed of apolymer, e.g., a substantially transparent polymer. After being formedinto the array of retroreflective cube-corner elements, the polymer ispreferably rigid, or substantially inflexible, at room temperature. Therigidity of the polymer in the array allows the cube-corner elements tomaintain their optical characteristics. The polymer can also benon-extensible, which is defined as not being capable of beingsubstantially stretched without breaking. The polymer can be selectedfrom a wide variety of polymers which include, but are not limited to,urethane, acrylic acid esters, cellulose esters, ethylenicallyunsaturated nitrites, hard epoxy acrylates, etc. Other polymers includepolycarbonates, polyesters and polyolefins, acrylate silanes, hardpolyester urethane acrylates. Other polymers, which are not as rigid,can also be used. These polymers include polyvinyl chloride andpolyvinylidene chloride. Preferably, the polymer is cast in a prismaticmold with a monomer or oligomer. The polymerization of the monomer oroligomer can be initiated by radiation, e.g., ultraviolet radiation.Retroreflective structures of the present invention can include an arrayof retroreflective cube-corner elements that does not need to containfire retardant additives in order to meet NFPA standards for theretroreflective structure. Consequently, in some embodiments, the arrayof cube-corner elements is essentially free of fire retardant additives.

In some embodiments, the polyvinyl chloride film and array ofretroreflective cube-corner elements can be formed by methods such asthose disclosed in U.S. Pat. No. 3,684,348, issued to Rowland on Aug.15, 1972; U.S. Pat. No. 3,689,346, issued to Rowland on Sep. 5, 1972;U.S. Pat. No. 3,811,983, issued to Rowland on May 21, 1974; U.S. Pat.No. 3,830,682, issued to Rowland on Aug. 20, 1974; U.S. Pat. No.3,975,083, issued to Rowland on Aug. 17, 1976; U.S. Pat. No. 4,332,847,issued to Rowland on Jun. 1, 1982; U.S. Pat. No. 4,801,193, issued toMartin on Jan. 31, 1989; U.S. Pat. No. 5,229,882, issued to Rowland onJul. 20, 1993; U.S. Pat. No. 5,236,751, issued to Martin, et al. on Aug.17, 1993; U.S. Pat. No. 5,264,063, issued to Martin on Nov. 23, 1992;U.S. Pat. No. 5,376,431, issued to Rowland on Dec. 27, 1994; U.S. Pat.No. 5,491,586, issued to Phillips on Feb. 13, 1996; U.S. Pat. No.5,512,219, issued to Rowland on Apr. 30, 1996; U.S. Pat. No. 5,558,740,issued to Bernard, et al. on Sep. 24, 1996; U.S. Pat. No. 5,592,330,issued to Bernard on Jan. 7, 1997; and U.S. Pat. No. 5,637,173, issuedto Martin, et al. on Jun. 10, 1997. The entire contents of each patentare incorporated herein by reference.

The cube-corner elements of the array can have a length along eachcube-side edge, for example, in the range of about 0.0015 to about 0.02inches (about 0.038 to about 0.51 mm). Preferably, each cube-side edgehas a length of about 0.003 to about 0.008 inches (about 0.076 to about0.2 mm) such as about 0.0035 to about 0.006 inches (about 0.089 to about0.15 mm). In one embodiment, each cube-side edge has a length of about0.0035 inches (about 0.089 mm). In general, retroreflective structurescontaining relatively small cube-corner elements are preferred. Withoutbeing held to any particular theory, retroreflective structurescontaining relatively small cube-corner elements are generally lessflammable than retroreflective structures containing larger cube-cornerelements.

The thickness of the array in the valleys where the cube-corner elementsintersect is preferably sufficiently thin so that the array can crackand split along the valleys when minimal force is applied to theretroreflective structure. In some embodiments, the thickness of thearray, which is the distance from the window side to apex of thecube-corner elements, is about 0.001 to about 0.009 inches (about 0.025to about 0.23 mm) such as about 0.001 to about 0.005 inches (about 0.025to about 0.13 mm), about 0.001 to about 0.003 inches (about 0.025 toabout 0.076 mm), or about 0.0015 to about 0.003 inches (about 0.038 toabout 0.076 mm). In one specific embodiment, the thickness of the arrayis about 0.0017 inches (about 0.043 mm).

In addition to the polyvinyl chloride film and the array ofretroreflective cube-corner elements, the retroreflective structuresalso include a flame retardant and heat resistant adhesive. Generally,the retroreflective structure includes flame retardant and heatresistant adhesive 18 underlying array of cube-corner elements 14.“Underlying” refers to the relative orientation of the retroreflectiveadhesive to the array of cube-corner elements.

Flame retardant and heat resistant adhesive 18 can be applied to prismfacets of the cube-corner elements for adhesion to fabric 20. If anadhesive is applied directly to the prism facets, however, the adhesivecan cause the surface of the prisms to wet, thereby destroying the airinterface and reducing, or even eliminating, the ability of the prismsto retroreflect. As a result, a reflective coating is preferably firstdeposited on the surface of the dihedral facets. Examples of suitablematerials for forming a reflective coating include, but are not limitedto, aluminum, silver, gold, palladium, and combinations thereof.Typically, the reflective coatings are formed by sputtering or by vacuumdeposition. For example, the cube-corner elements can be vapor depositedwith aluminum to create a reflective metal layer. In one embodiment,aluminum is vapor deposited whereby aluminum is heated under a vacuumand aluminum vapor is condensed onto the cube-corner elements to form aaluminum layer, e.g., a continuous aluminum layer. Alternatively, metallacquers, dielectric coatings and other specular coating materials canbe employed to form a reflective coating on the cube-corner elements.The thickness of the aluminum layer can be in the range of about 200 toabout 600 Angstroms, for example, about 200 to about 500 or about 200 toabout 400 Angstroms. In one embodiment, adhesive is applied directly toa metallized surface of the array of cube-corner elements.

Adhesive 18 can be selected based on its ability to adhesively bond toboth the fabric and to the array of cube-corner elements, e.g., an arrayof metallized cube-corner elements. In addition, the adhesive shouldprovide enough adhesive strength such that the array of cube-cornerelements does not separate from the polyvinyl chloride film or from thefabric after laundering or usage. Additionally, the adhesive shouldprovide flame retardancy as well as heat resistance to theretroreflective structure. Heat resistance can be defined as notmelting, dripping, igniting, or separating after the sample is placed ina 260° C. oven for 5 minutes as specified by the National FireProtection Association (NFPA) EN471 specification. Flame retardancy canbe defined as having less than 2 seconds of afterflame after the samplehas been vertically burned in accordance with the NFPA EN471specification.

Adhesive 18 can include silicone adhesives and acrylic adhesives such asacrylic-based pressure sensitive adhesives or silicone pressuresensitive adhesives. In one preferred embodiment, the adhesive is anacrylic-based adhesive due to its wide availability and relatively lowcost. In general, acrylic adhesives have excellent UV resistance,excellent resistance to non-polar solvents and therefore make anexcellent choice for this application. However, not all acrylicadhesives exhibit high temperature resistance. An example of awell-known method to increase the heat resistance is to crosslink theadhesive. Crosslinking the adhesive can reduce the mobility of theacrylic molecules and therefore can provide excellent heat resistance tothe retroreflective structure by reducing, or preventing, melting and/ordripping at high temperatures. In a preferred embodiment, the adhesiveis a crosslinked acrylic pressure sensitive adhesive. A two-stagecrosslinking system is generally preferred. In this embodiment, a firstcrosslinking stage allows partial crosslinking while still maintainingimportant adhesive properties such as, for example, tack. This usuallyoccurs at drying temperatures during coating of a solvent-basedadhesive. The second crosslinking stage can occur at higher temperatureto allow the adhesive to crosslink in application such that the adhesivedoes not melt or drip during high temperature exposure. In someembodiments, the second crosslinking stage includes a melamine or epoxysystem.

The thickness of the adhesive can be about 0.001 inches (about 0.025 mm)to about 0.008 inches (about 0.2 mm) such as about 0.002 inches (0.051mm) to about 0.006 inches (about 0.15 mm), about 0.002 inches (0.051 mm)to about 0.0045 inches (0.11 mm), about 0.003 inches (about 0.076 mm) toabout 0.004 inches (about 0.1 mm), or about 0.0035 inches (about 0.089mm).

Acrylic adhesives can be flammable. Thus, it can be necessary tointroduce flame retardant additives into the adhesive. The mosteffective flame retardant systems include halogen-based additives suchas brominated or chlorinated additives. In one embodiment, the flameretardant and heat resistant adhesive contains at least one additiveselected from the group consisting of flame retardant chlorinatedadditives, flame retardant brominated additives, and combinationsthereof. Synergists such as antimony trioxide, antimony pentoxide,sodium antimonite, zinc borate and combinations thereof can be used toimprove the flame retardancy of the adhesive. Thus, in some embodiments,the flame retardant and heat resistant adhesive contains at least oneflame retardant synergist selected from the group consisting of antimonytrioxide, antimony pentoxide, sodium antimonite, zinc borate, andcombinations thereof. Other flame retardant systems such asphosphorous-based additives, boron based additives, aluminumtrihydroxide, nitrogen-based additives and combinations thereof can alsobe included in the adhesive. A preferred flame retardant system is ahalogenated flame retardant coupled with an antimony trioxide synergist.

Flame retardant and heat resistant adhesives can be obtained from avariety of sources. One example of a suitable acrylic adhesive wasobtained from Syntac Coated Products, LLC (Bloomfield, Conn.). Thisacrylic adhesive is a two-stage crosslinked acrylic adhesive. The firststage crosslinks during coating of the adhesive when the solvent isevaporated to leave a solid coating. The second stage crosslinkingoccurs between about 200 and about 250° F. (between about 93 and about121° C.). This particular adhesive uses an epoxy secondary crosslinkingsystem.

In another embodiment, a nitrile rubber/phenolic blend adhesive can beused such as a nitrile rubber/phenolic blend adhesive which crosslinksat a high temperature. One example of a nitrile rubber/phenolic blendadhesive is H206U available from Scapa North America (Windsor, Conn.).Nitrile rubber/phenolic blend adhesives can also include flame retardantadditives such as described supra.

In one aspect, the present invention includes a transparent plasticizedpolyvinyl chloride film, an array of retroreflective cube-cornerelements underlying the transparent plasticized polyvinyl chloride film,a polymeric film layer sealed through the array of cube-corner elementsto the transparent plasticized polyvinyl chloride film, a flameretardant and heat resistant adhesive underlying the array ofretroreflective cube-corner elements, and a flame retardant woven fabricbonded to the flame retardant and heat resistant adhesive. In oneembodiment, the flame retardant and heat resistant adhesive is bonded tothe polymeric film layer and also to the flame retardant woven fabric.The polymeric film layer can be, for example, a plasticized polyvinylchloride film. The composition of such a polymeric film layer can besimilar to transparent plasticized polyvinyl chloride film 12 describedsupra. Polymeric film layer, however, can be transparent or opaque.Polymeric film layer can be sealed through the array of cube-cornerelements to the transparent plasticized polyvinyl chloride film throughtechniques such as, for example, radio frequency or ultrasonic sealingor welding. In some embodiments, such a polymeric film layer caneliminate any need for metallization of the cube-corner elements.

The retroreflective structures of the present invention also include aflame retardant woven fabric bonded to the flame retardant and heatresistant adhesive. Many flame retardant woven fabrics are suitable.Flame retardant woven fabric 20 can include, for example, glass fiberfabric, modacrylic fabrics, modacrylic fabric, Nomex fabric, Nomex andKevlar blends, polybenzimidizole fabric, woven corespun composite yarnwith a glass fiber core and a sheath of cotton and flame retardantmodacrylic fiber. In some embodiments, the flame retardant woven fabricis selected from the group consisting of fiber glass fabrics, flameretardant modacrylic fabrics, Nomex fabrics, Nomex-Kevlar fabrics,polybenzimidizole fabrics, fabrics which include a corespun compositeyarn with a glass fiber core and a sheath of cotton and flame retardantmodacrylic fiber, and combinations thereof. In one preferred embodiment,the fabric is composed of a corespun composite yarn with a glass fibercore and a sheath of cotton and flame retardant modacrylic fibersurrounding and covering the core in both the warp and fill directionsof the fabric.

The fabric can include glass fiber and flame retardant modacrylic fiber.For example, the woven fabric can include about 20 to about 90 weightpercent glass fiber such as about 25 to about 80, about 30 to about 70,about 30 to about 60, or about 35 to about 45 weight percent glassfiber. The woven fabric can include, for example, about 5 to about 80weight percent modacrylic fiber such as about 10 to about 70, about 15to about 50, or about 20 to about 30 weight percent modacrylic fiber.The fabric can also include blends of cotton fiber. In some embodiments,the woven fabric includes no more than about 60 weight percent cottonfiber such as, for example, no more than about 50, about 40, or about 30weight percent cotton fiber. For example, the fabric can about 10 toabout 50 weight percent cotton fiber such as about 20 to about 40 orabout 30 to about 40 weight percent cotton fiber. In specificembodiments, the woven fabric includes about 35 to about 45 weightpercent glass fiber, about 30 to about 40 weight percent cotton fiber,and about 20 to about 30 weight percent modacrylic fiber. For example,the woven fabric can include about 40% glass fiber, about 35% cotton,and about 25% modacrylic fiber (all by weight). In other embodiments,the woven fabric includes about 35 to about 45 weight percent glassfiber and about 55 to about 65 weight percent modacrylic fiber. Forexample, the woven fabric can include about 41 weight percent glassfiber and about 59 weight percent modacrylic fiber.

Modacrylic fiber is an acrylic synthetic fiber made from a polymercomprising primarily acrylonitrile. Modacrylics are generally made fromcopolymers of polyacrylonitrile and other polymers such as vinylchloride, vinylidene chloride, vinyl bromide, or vinylidene bromide. Anexample of modacrylic fiber suitable for use in the present invention isavailable commercially under the trademark PROTEX® C from Kaneka AmericaCorporation (New York, N.Y.).

The fabric utilized in the present invention can provide flameretardancy; tear resistance, heat resistance, and dimensional stabilityto the retroreflective structure. The weight of the fabric can be, forexample, about 1 to about 15 ounces/square yard (oz/yd²) (about 34 toabout 510 grams/square meter (g/m²)) such as about 2 to about 10 oz/yd²(about 68 to about 340 g/m²), about 3 to about 8 oz/yd² (about 100 toabout 270 g/m²), or about 3 to about 6 oz/yd² (about 100 to about 200g/m²). In one embodiment, the fabric has an relatively open weave toallow the adhesive to penetrate into the fabric for desired adhesion tothe fabric. For example, the woven fabric can have a weave density ofabout 40 to about 70 (Warp) by about 25 to about 45 (Fill) threads perinch (per 25.4 mm) such as the woven fabric has a weave density of about55 to about 65 (Warp) by about 30 to about 40 (Fill) threads per inch(per 25.4 mm). In some embodiments, the fabric has a weave density ofless than about 60 (Warp) by about 35 (Fill) threads per inch (per 25.4mm).

An example of a suitable woven fabric is 5.7 oz/yd² (about 190 g/m²)core spun composite fabric having a glass fiber core with a sheath ofcotton and flame retardant modacrylic and containing about 40 weightpercent glass fiber, about 35 weight percent cotton, and about 25 weightpercent modacrylic fiber, and having a weave density of about 60 (Warp)by about 35 (Fill) threads per inch (per 25.4 mm). Such a fabric isavailable from Spring Industries, Inc. (Fort Mill, S.C.) under theFIREGARD® trademark. Another example of a suitable woven fabric includesabout 41 weight percent glass fiber and about 59 weight percent flameretardant modacrylic fiber with a weave density of about 44 (Warp) byabout 34 (Fill) threads per inch (per 25.4 mm). Such a fabric is alsoavailable from Spring Industries, Inc. (Style No. 4-7091-114) under theFIREGARD® trademark.

Examples of fabrics suitable for use in the present invention includethose described in U.S. Pat. No. 4,921,756 issued to Tolbert, et al. onMay 1, 1990; U.S. Pat. No. 6,146,759 issued to Land on Nov. 14, 2000;U.S. Pat. No. 6,287,690 issued to Land on Sep. 11, 2001; U.S. Pat. No.6,410,140 issued to Land, et al. on Jun. 25, 2002; U.S. Pat. No.6,553,749 issued to Land, et al. on Apr. 29, 2003; U.S. Pat. No.6,606,846 issued to Land on Aug. 19, 2003; and U.S. Pat. No. 5,540,980issued to Tolbert, et al. on Jul. 30, 1996., the entire contents of eachof which is incorporated herein by reference. For example, U.S. Pat. No.4,921,756 describes a fire resistant nonlively corespun yarn for use informing fire resistant fabrics and lightweight substrates for coatedfabrics, the nonlively corespun yarn comprising an air jet spun unpliedyarn without any appreciable S or Z twist and having a core of hightemperature resistant continuous filament fiberglass, and a sheath oflow temperature resistant staple fibers surrounding and covering thecore.

It can be important that the fabric be free of any coatings such as, forexample, sizing agents that can affect the bond of the adhesive to thefabric. Common sizing agents include starch based and synthetic polymerssuch as polyacrylic acid ester, polyvinyl alcohol, and acrylic.Typically, sizing agents are required to protect warp yarns againstabrasion during weaving. However, sizing agents can be removed through ade-sizing operation to maximize the adhesion of the adhesive to thefabric. Thus, in some embodiments, the woven fabric is essentiallyde-sized of any sizing agents such as sizing agents that may have beenutilized during weaving. For example, the woven fabric can beessentially free of starch-based and synthetic polymers such aspolyacrylic acid ester, polyvinyl alcohol, and acrylic.

In one aspect, retroreflective structures of the present inventioninclude a transparent plasticized polyvinyl chloride film; an array ofretroreflective cube-corner elements underlying the transparentplasticized polyvinyl chloride film; a metallized reflective layerdeposited on the retroreflective cube-corner elements; a flame retardantand heat resistant crosslinked acrylic adhesive bonded to the metallizedreflective layer; and a flame retardant woven fabric bonded to theacrylic adhesive. Suitable transparent plasticized polyvinyl chloridefilms, metallized reflective layers, flame retardant and heat resistantcrosslinked acrylic adhesives, and flame retardant woven fabric aredescribed supra.

In some embodiments, one or more optional transparent coatings, forexample, transparent coatings 24 and 26, are applied adjacent topolyvinyl chloride film 12. For example, retroreflective structure 22can include transparent coatings on both sides of polyvinyl chloridefilm 12. Alternatively, the retroreflective structure can include atransparent coating on only one side of the polyvinyl chloride film. Inone embodiment, the array of retroreflective cube-corner elements can beformed on the surface of transparent coating 26.

Preferably, coating formulations for transparent coatings are selectedsuch that the resulting coatings are flexible, provide a strong bond tothe plasticized polyvinyl chloride film, and provide a strong bond toany optional printed ink layers (described infra). For instances inwhich the retroreflective structure includes two or more transparentcoatings, the transparent coatings can have the same or differentcompositions. Transparent coatings can be applied by applying variouscoating formulations over the polyvinyl chloride film. For example, thecoating formulation can be a radiation curable formulation, a solventbased coating formulation, or a water based coating formulation.

In one embodiment, the base chemical for a transparent coating is aurethane acrylate prepolymer. Suitable coating formulations can include,for example, one or more of the following prepolymers: aliphaticurethane acrylates, aliphatic urethane methacrylates, aromatic urethaneacrylates, aromatic urethane methacrylates, imide/ester/amide urethaneacrylates, phenoxy urethane acrylates, phenoxy urethane methacrylates,polyester acrylates, polyester methacrylates, chlorinated polyesteracrylates, chlorinated polyester methacrylates, dendritic polyesteracrylates, dendritic polyester methacrylates, epoxy acrylates, epoxymethacrylates, polybutadiene acrylates, and polybutadiene methacrylates.In a preferred embodiment, the base chemical for the coating is analiphatic urethane acrylate prepolymer. Generally, the molecular weightof the prepolymer is desired to be greater than 500 grams/mol, however,in some embodiments, the molecular weight of the prepolymer can be lessthan 500 grams/mol. In a preferred embodiment, the molecular weight ofthe prepolymer is between 500 and 3000 grams/mol. In some embodiments,the prepolymer has an acrylate moiety functionality, for example, ofbetween 1 and 6 such as between 1.2 and 3.

The transparent coating formulations also can contain other prepolymersfor such functions as viscosity modification, adhesion promotion, tackreduction, and other purposes. Examples of monofunctional prepolymersthat can be used for viscosity modification include but are not limitedto isobornyl acrylate, 2(2-ethoxyethoxy) ethyl acrylate, tridecylacrylate, octyldecyl acrylate, 2-phenoxyethyl acrylate, 2-phenoxyethylmethacrylate, alkoxylated lauryl acrylate, lauryl acrylate, laurylmethacrylate, isodecyl acrylate, stearyl acrylate, and stearylmethacrylate. Examples of multifunctional prepolymers that can be usedfor viscosity modification include, but are not limited to,trimethylolpropane triacrylate, trimethylolpropane trimethacrylate,ethoxylated trimethylolpropane trimethacrylate, propoxylatedtrimethylolpropane triacrylate, and propoxylated glyceryl triacrylate.Additional prepolymers that can be used for additional functionalbenefits include, but are not limited to, epoxy acrylates, brominatedepoxy acrylates, polyester acrylates, silicone acrylates,fluoroacrylates and polybutadiene acrylates.

In some embodiments, the transparent coatings are radiation curable. Ingeneral, a photoinitiator is needed to cure such a coating formulation.Examples of photoinitiators that can be used include, but are notlimited to, benzyldimethylketal,2-hydroxy-2-methyl-1-phenyl-1-propanone, alpha-hydroxycylohexylphenylketone, benzophenone, 2,4,6-trimethylbenzoylphenyl phosphineoxide,isopropylthioxanthone, ethyl-4-dimethylammino benzoate,2-ethyl-4-dimethyl amino benzoate, oligo[2-hydroxy-2-methyl-1-[4-(1-methylvinyl)phenyl]propanone], difunctionalalpha-hydroxy ketone, 1-[4-94-benzoylphenylsulfanyl)phenyl]-2-methyl-2-(4-methylphenylsulfonyl) propan-1-one,2-methyl-1[4-(methylthio)phenyl]-2-morpholinopropane-1-one,phenylbis(2,4,6-trimethylbenzoyl)-phosphine oxide),2,2-dimethoxy-1,2-diphenylethan-1-one, and combinations thereof.

Since many of the above-mentioned acrylate prepolymers can be flammable,in some instances thin transparent coatings are used. In someembodiments, the retroreflective structure includes one or moretransparent coatings with a thickness of about 0.0001 inch (about 0.0025mm) to about 0.0008 inch (about 0.02 mm), such as about 0.0001 inch(about 0.0025 mm) to about 0.0005 inch (about 0.013 mm), about 0.0001inch (about 0.0025 mm) to about 0.0003 inch (about 0.0076 mm), or about0.0002 inch (about 0.0051 mm). In addition, or alternatively, flameretardant additives may be included in the transparent coating. Flameretardant additives and methods for incorporating them into coatings arewithin the knowledge of those skilled in the art.

In some instances, the retroreflective structure can also include aprinting ink, such as an opaque white printing ink. A printing ink canbe included in the retroreflective structures, for example, to helpachieve appropriate Cap Y to meet industry whiteness specifications.Printing ink can be applied, for example, between the polyvinyl chloridefilm 12 and a transparent coating. Alternatively, printing ink can beapplied between a transparent coating and the array of retroreflectivecube-corner elements. For example, printing ink can be applied betweentransparent coating 24 and retroreflective cube-corner element array 14.Printing ink can enhance Cap Y performance, however, it also can reducethe retroreflectivity of the prisms it covers. Therefore, the printingink is often non-continuous. The printing ink can take various forms.For example, the printing ink can be in the form of a pattern, logo,lettering, etc. In some embodiments, the printing ink has been appliedusing a screen printing method.

In some embodiments, a retroreflective structure includes a transparentplasticized polyvinyl chloride film having a first side and a secondside, a transparent radiation cured coating attached to the first sideof the transparent plasticized polyvinyl chloride film, a non-continuouswhite opaque printed layer formed on the first side of the transparentplasticized polyvinyl chloride film, an array of retroreflective cubecorner elements attached to the white opaque printed layer, a metallizedreflective layer formed on the retroreflective cube corner elements, aflame retardant high temperature adhesive laminated to the metallizedreflective layer, and a flame retardant woven fabric laminated to theflame retardant high temperature adhesive.

A method for manufacturing a retroreflective structure includesattaching a transparent plasticized polyvinyl chloride film to an arrayof retroreflective cube-corner elements and attaching a flame retardantwoven fabric to the array of retroreflective cube-corner elements usinga flame retardant and heat resistant adhesive. In some embodiments, ametallized reflective layer is deposited on the retroreflectivecube-corner elements prior to attaching the flame retardant woven fabricto the array of retroreflective cube-corner elements using the flameretardant and heat resistant adhesive.

In another method for manufacturing a retroreflective structure, atransparent coating layer (e.g., a radiation cured transparent coating)is applied to a first side of a transparent plasticized polyvinylchloride film. A non-continuous white opaque printing ink is attached tothe transparent coating layer. An array of retroreflective elements isthen attached to the white opaque printing ink. A metallized reflectivelayer is applied to an array of retroreflective cube-corner elements,thereby forming metallized retroreflective cube-corner elements. Lastly,a flame retardant heat resistant adhesive is coated to a flame retardantwoven fabric and laminated to the metallized retroreflective cube-cornerelements.

The retroreflective structures of the present invention can be attachedto a suitable article of clothing such as a firefighter's overcoat, orother structure such as a fire helmet or air tank, by techniques knownin the art. For instance, a retroreflective structure can be attached byan adhesive such as a plasticizer-resistant, pressure-sensitive orheat-activated adhesive. Alternatively, retroreflective structures canbe sewn onto clothing.

EXEMPLIFICATION Example 1

This Example describes a flame retardant and heat resistantretroreflective structure made in accordance with the present invention.

An array of retroreflective cube corner elements was attached to an0.008 inch (about 0.2 mm) plasticized PVC film. A flame retardant, hightemperature acrylic pressure sensitive adhesive with a thickness of0.0035 inches (about 0.089 mm) was applied to the retroreflective cubecorner elements. The adhesive used was RA196FR (Syntac Coated Products,LLC; New Hartford, Conn.). FIREGARD® fabric (Spring Industries, Inc.;Fort Mill, S.C.) was laminated to the pressure sensitive adhesive. Thefabric was composed of a weave of corespun composite yarn with a glassfiber core and a sheath of cotton and flame retardant modacrylicsurrounding and covering the core in both the warp and fill directionsof the fabric. The overall blend of the woven fabric was 41% glassfiber, 35% cotton, and 25% modacrylic fiber. The fabric had a weavedensity of 52 (warp)×36 (fill) threads per inch (per 25.4 mm) in a plainweave configuration and a fabric weight was 4.7 oz/yd² (about 160 g/m²).

Example 2

This Example describes a retroreflective structure similar to thestructure of Example 1 but made with a non-flame retardant and non-hightemperature adhesive.

An array of retroreflective cube corner elements was attached to an8-mil plasticized PVC film. Scapa Unifilm U604X acrylic pressuresensitive adhesive (Scapa North America; Windsor, Conn.) with athickness of 0.0035 inches (about 0.089 mm) was applied to theretroreflective cube corner elements. As in Example 1, FIREGARD® fabric(Spring Industries, Inc.) was laminated to the pressure sensitiveadhesive.

Example 3

This Example describes a retroreflective structure similar to thestructure of Example 1 but made using an all cotton woven fabric.

An array of retroreflective cube corner elements was attached to an0.008 inch (about 0.2 mm) plasticized PVC film. A flame retardant, hightemperature acrylic pressure sensitive adhesive, RA196FR (Syntac CoatedProducts, LLC; New Hartford, Conn.), with a thickness of 0.0035 inches(about 0.089 mm) was applied to the retroreflective cube cornerelements. 100% cotton fabric was laminated to the pressure sensitiveadhesive. The cotton fabric had a weave density of 80 (warp)×48 (fill)in a twill weave configuration and a fabric weight of 8.7 oz/yd² (about290 g/m²)

Example 4

This Example describes testing performed on retroreflective structuresthat were formed as described in Examples 1-3.

Testing was conducted in accordance with NFPA 1971, Standard onProtective Ensembles for Structural Fire Fighting and Proximity FireFighting (2007 Ed.), Flame Resistance Test (§ 8.2) and 260° C. Heat Test(§ 8.6.4.1). Table 1 shows results of flame resistance testing. Table 2shows results of the 260° C. Heat Test.

TABLE 1 After Flame (seconds) Char Length (millimeters) RetroreflectiveStructure of Example 1 0.84 7 1.46 7 1.12 8 1.31 11 1.03 9Retroreflective Structure of Example 2 62 Not Applicable*Retroreflective Structure of Example 3 48.84 38 3.84 48 5.40 35 2.34 672.87 47 *The entire retroreflective structure of Example 2 combusted,failing the test.

TABLE 2 Retroreflective Structure Pass/Fail Comments Example 1 PASS Thesample did not melt, drip, ignite, or separate. Example 2 FAIL Thesample did not melt, drip, or ignite. The sample separated between theadhesive and the prisms. Example 3 PASS The sample did not melt, drip,ignite or separate.

Based on the 260° C. Heat Test (§ 8.6.4.1) and Flame Resistance Test (§8.2), the retroreflective structure containing both a corespun compositeyarn and a flame retardant, high temperature acrylic adhesive had thebest performance, passing both tests. The retroreflective structure madewith an all cotton woven fabric, Example 3, had the worst performance,failing both tests.

While this invention has been particularly shown and described withreferences to preferred embodiments thereof, it will be understood bythose skilled in the art that various changes in form and details may bemade therein without departing from the scope of the inventionencompassed by the appended claims.

1. A retroreflective structure, comprising: a) a transparent plasticizedpolyvinyl chloride film; b) an array of retroreflective cube-cornerelements underlying the transparent plasticized polyvinyl chloride film;c) a flame retardant and heat resistant adhesive underlying the array ofretroreflective cube-corner elements; and d) a flame retardant wovenfabric bonded to the flame retardant and heat resistant adhesive,wherein the flame retardant and heat resistant adhesive (c) contains atleast one flame retardant synergist selected from the group consistingof antimony trioxide, antimony pentoxide, sodium antimonite, zincborate, and combinations thereof.
 2. The retroreflective structure ofclaim 1 wherein the transparent plasticized polyvinyl chloride film hasa Shore A hardness of about 30 to about
 45. 3. The retroreflectivestructure of claim 1 wherein the transparent plasticized polyvinylchloride film has a thickness of about 0.001 to about 0.022 inches(about 0.025 to about 0.56 mm).
 4. The retroreflective structure ofclaim 1 wherein the transparent plasticized polyvinyl chloride film hasa thickness of about 0.006 to about 0.018 inches (about 0.15 to about0.46 mm).
 5. The retroreflective structure of claim 1 wherein thetransparent plasticized polyvinyl chloride film includes a fluorescentdye.
 6. The retroreflective structure of claim 1 wherein the array ofretroreflective cube corner elements is coated with a metal.
 7. Theretroreflective structure of claim 6 wherein the metal is selected fromthe group consisting of aluminum, silver, gold, and palladium.
 8. Theretroreflective structure of claim 1 wherein the flame retardant andheat resistant adhesive is selected from the group consisting ofsilicone adhesives and acrylic adhesives.
 9. The retroreflectivestructure of claim 1 wherein the flame retardant and heat resistantadhesive is a crosslinked acrylic adhesive.
 10. The retroreflectivestructure of claim 1 wherein the flame retardant and heat resistantadhesive contains at least one additive selected from the groupconsisting of flame retardant chlorinated additives, flame retardantbrominated additives, and combinations thereof.
 11. The retroreflectivestructure of claim 1 wherein the flame retardant woven fabric isselected from the group consisting of fiber glass fabrics, flameretardant cotton fabrics, flame retardant modacrylic fabrics, Nomexfabrics, Nomex-Kevlar fabrics, polybenzimidizole fabrics, fabrics whichinclude a corespun composite yarn with a glass fiber core and a sheathof cotton and flame retardant modacrylic fiber, and combinationsthereof.
 12. The retroreflective structure of claim 1 wherein the wovenfabric has a weave density of about 40 to about 70 (Warp)×about 25 toabout 45 (Fill) threads per inch (per 25.4 mm).
 13. The retroreflectivestructure of claim 1 wherein the woven fabric has a weave density ofabout 55 to about 65 (Warp)×about 30 to about 40 (Fill) threads per inch(per 25.4 mm).
 14. The retroreflective structure of claim 1 wherein thewoven fabric is essentially de-sized of any sizing agents that may havebeen utilized during weaving.
 15. The retroreflective structure of claim1 wherein the fabric includes a core spun composite yarn with a glassfiber core and a sheath of cotton and flame retardant modacrylic fiber.16. The retroreflective structure of claim 15 wherein the woven fabricincludes about 30 to about 60 weight percent glass fiber.
 17. Theretroreflective structure of claim 15 wherein the woven fabric includesno more than about 40 weight percent cotton fiber.
 18. Theretroreflective structure of claim 15 wherein the woven fabric includesabout 10 to about 70 weight percent modacrylic fiber.
 19. Theretroreflective structure of claim 15 wherein the woven fabric includesabout 35 to about 45 weight percent glass fiber, about 30 to about 40weight percent cotton fiber, and about 20 to about 30 weight percentmodacrylic fiber.
 20. The retroreflective structure of claim 1 furtherincluding a polymeric film layer sealed through the array of cube-cornerelements to the transparent plasticized polyvinyl chloride film.
 21. Theretroreflective structure of claim 20 wherein the flame retardant andheat resistant adhesive is bonded to the polymeric film layer and alsoto the flame retardant woven fabric.
 22. The retroreflective structureof claim 1, further including a layer of printing ink overlying thetransparent plasticized polyvinyl chloride film.
 23. The retroreflectivestructure of claim 1, further including a layer of printing inkunderlying the transparent plasticized polyvinyl chloride film.
 24. Theretroreflective structure of claim 1, further including a layer ofprinting ink overlying the array of retroreflective cube-cornerelements.
 25. A retroreflective structure, comprising: a) a transparentplasticized polyvinyl chloride film; b) an array of retroreflectivecube-corner elements underlying the transparent plasticized polyvinylchloride film; c) a metallized reflective layer deposited on theretroreflective cube-corner elements; d) a flame retardant and heatresistant crosslinked acrylic adhesive bonded to the metallizedreflective layer; and e) a flame retardant woven fabric bonded to theacrylic adhesive, wherein the acrylic adhesive (d) contains at least oneflame retardant synergist selected from the group consisting of antimonytrioxide, antimony pentoxide, sodium antimonite, zinc borate, andcombinations thereof.
 26. The retroreflective structure of claim 25wherein the transparent plasticized polyvinyl chloride film has a ShoreA hardness of about 30 to about
 45. 27. The retroreflective structure ofclaim 25 wherein the transparent plasticized polyvinyl chloride film hasa thickness of about 0.001 to about 0.022 inches (about 0.025 to about0.56 mm).
 28. The retroreflective structure of claim 25 wherein thetransparent plasticized polyvinyl chloride film has a thickness of about0.006 to about 0.018 inches (about 0.15 to about 0.46 mm).
 29. Theretroreflective structure of claim 25 wherein the transparentplasticized polyvinyl chloride film includes a fluorescent dye.
 30. Theretroreflective structure of claim 25 wherein the metallized reflectivelayer includes at least one metal selected from the group consisting ofaluminum, silver, gold, and palladium.
 31. The retroreflective structureof claim 25 wherein the metallized reflective layer is an aluminumlayer.
 32. The retroreflective structure of claim 25 wherein the acrylicadhesive includes at least one additive selected from the groupconsisting of flame retardant chlorinated additives, brominatedadditives, and combinations thereof.
 33. The retroreflective structureof claim 25 wherein the flame retardant woven fabric is selected fromthe group consisting of fiber glass fabrics, flame retardant cottonfabrics, flame retardant modacrylic fabrics, Nomex fabrics, Nomex-Kevlarfabrics, polybenzimidizole fabrics, fabrics which include a corespuncomposite yam with a glass fiber core and a sheath of cotton and flameretardant modacrylic fiber, and combinations thereof.
 34. Theretroreflective structure of claim 25 wherein the flame retardant wovenfabric includes a corespun composite yarn with a glass fiber core and asheath of cotton and flame retardant modacrylic fiber.
 35. Theretroreflective structure of claim 25 wherein the woven fabric has aweave density of about 40 to about 70 (Warp)×about 25 to about 45 (Fill)threads per inch (per 25.4 mm).
 36. The retroreflective structure ofclaim 25 wherein the woven fabric is essentially de-sized of any sizingagents that may have been utilized during weaving.
 37. Theretroreflective structure of claim 25, further including a layer ofprinting ink overlying the transparent plasticized polyvinyl chloridefilm.
 38. The retroreflective structure of claim 25, further including alayer of printing ink underlying the transparent plasticized polyvinylchloride film.
 39. The retroreflective structure of claim 25, furtherincluding a layer of printing ink overlying the array of retroreflectivecube-corner elements.